WO2014186386A1 - Procédés de synthèse de l'acide acétique par oxydation de l'éthane - Google Patents

Procédés de synthèse de l'acide acétique par oxydation de l'éthane Download PDF

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Publication number
WO2014186386A1
WO2014186386A1 PCT/US2014/037886 US2014037886W WO2014186386A1 WO 2014186386 A1 WO2014186386 A1 WO 2014186386A1 US 2014037886 W US2014037886 W US 2014037886W WO 2014186386 A1 WO2014186386 A1 WO 2014186386A1
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Prior art keywords
acetic acid
acid composition
purified
weight
ethane
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PCT/US2014/037886
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English (en)
Inventor
Mustapha N. KARIME
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Saudi Basic Industries Corporation
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Application filed by Saudi Basic Industries Corporation filed Critical Saudi Basic Industries Corporation
Priority to AU2014265570A priority Critical patent/AU2014265570B2/en
Priority to CN201480026054.3A priority patent/CN105209418B/zh
Priority to US14/787,661 priority patent/US9738585B2/en
Priority to CA2907955A priority patent/CA2907955A1/fr
Priority to EP14730034.7A priority patent/EP2997003A1/fr
Priority to JP2016514040A priority patent/JP2016523834A/ja
Priority to KR1020157031220A priority patent/KR20160005696A/ko
Publication of WO2014186386A1 publication Critical patent/WO2014186386A1/fr

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/42—Separation; Purification; Stabilisation; Use of additives
    • C07C51/43—Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
    • C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
    • C07C51/215—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of saturated hydrocarbyl groups

Definitions

  • the present disclosure and invention relate to methods for the preparation of acetic acid via the oxidation of ethane, including the preparation of high purity acetic acid that comprises very low concentrations of formic acid impurity.
  • ethane is common in nature and can be isolated on an industrial scale during the purification of natural gas or as a byproduct of various petroleum refining processes, such as from catalytic cracking of higher hydrocarbons.
  • the value and/or price of ethane is, however, currently relatively low, either as a fuel, or as a potential feedstock for making other petrochemicals such as ethylene, or acetic acid.
  • Acetic acid CH 3 -CO 2 H
  • CH 3 -CO 2 H is a worldwide commodity produced at the level of hundreds of millions of tons per year, as a precursor for vinyl acetate monomer and polymers, and for making various acetate ester solvents and other chemicals.
  • many processes for making acetic acid have been developed and commercially employed over the years, acetic acid production by methanol carboxylation is currently dominant in the chemicals industry.
  • ethane oxidation processes produce fewer kinds and quantities of impurities heavier than ethanol
  • ethane oxidation processes also tend to produce relatively high quantities of formic acid, which because of its chemical and physical properties that are similar to acetic acid, is very difficult to separate from acetic acid, particularly to produce very high purity acetic acid containing very low levels of formic acid.
  • Even low levels of formic acid in acetic acid are undesirable because the formic acid promotes corrosion of metal vessels used to make and store acetic acid.
  • the present invention in some aspects, satisfies these and other needs, by providing methods for purifying acids.
  • methods for purifying acrylic acid and/or acetic acid are provided.
  • the invention is directed towards a method for producing acetic acid comprising: producing a crude acetic acid composition comprising formic acid from ethane via ethane oxidation; and then purifying the crude acetic acid composition by crystallization to remove formic acid to achieve a purified acetic acid composition;
  • the formic acid is present in the purified acetic acid composition in an amount less than 0.2 % by weight, based on the total weight of the purified acetic acid composition.
  • the Figure shows a phase diagram for the crystallization of acetic acid / water mixtures over a range of acetic acid weight percentages and crystallization temperatures.
  • Ranges can be expressed herein as from “about” one particular value, and/or to "about” another particular value.
  • about can mean the value itself plus or minus about 10% of that particular value, unless another meaning is specified herein, or such a meaning is clearly inappropriate to one of ordinary skill in the art.
  • another aspect includes from the one particular value and/or to the other particular value.
  • values are expressed as approximations, by use of the antecedent "about,” it will be understood that the particular value forms another aspect. It will be further understood that the endpoints of each of the ranges are significant both in relation to the other endpoint, and independently of the other endpoint.
  • X and Y are present at a weight ratio of 2:5, and are present in such ratio regardless of whether additional components are contained in the compound.
  • a weight percent of a component is based on the total weight of the formulation or composition in which the component is included.
  • the various aspects of the multiple methods for producing acetic acid described herein do however comprise at least two as shown above, and can also encompass additional steps, and/or limitations as further described in the written description below and dependent claims written below.
  • the ethane oxidation is performed in the gas phase from gaseous reactants (ethane and oxygen or air), and initially produces a mixture of reactor product steam vapors, which include some gaseous products (such as unreacted ethane and/or oxygen, ethylene, carbon monoxide, carbon dioxide) along with some reaction product vapors that can be readily condensed to liquid form (for example acetic acid, formic acid, and water).
  • gaseous reactants ethane and oxygen or air
  • some reaction product vapors that can be readily condensed to liquid form (for example acetic acid, formic acid, and water).
  • the crude acetic acid formic acid, and water
  • composition is a liquid that comprises liquid acetic acid as a major component.
  • the various processes described herein typically include one or more of a wide variety of possible steps intermediate between these steps to separate crude acetic acid in liquid form from the reactor product stream vapors. Accordingly, many aspects of the invention include an intermediate step of separating acetic acid from a reactor product steam produced by the ethane oxidation to form the crude acetic acid composition. In some aspects, the ethane oxidation utilizes 0 2 and/or air as an oxidant.
  • the crude acetic acid composition is then purified by crystallization of acetic acid from the crude acetic acid composition, typically at low temperatures, to in order to remove water and/or organic impurities and to achieve the purified acetic acid composition.
  • the formic acid is present in the purified acetic acid composition in an amount less than about 0.2 %, or less than about 0.1%, or less than about 0.05%, or less than about 0.03%, or less than about 0.01% by weight, based on the total weight of the purified acetic acid composition.
  • Described herein are methods for producing acetic acid comprising the steps of: producing a crude acetic acid composition comprising formic acid from ethane via ethane oxidation; and then purifying the crude acetic acid composition by crystallization to remove formic acid to achieve a purified acetic acid composition; wherein the formic acid is present in the purified acetic acid composition in an amount less than 0.2 % by weight, based on the total weight of the purified acetic acid composition.
  • the method comprises producing a crude acetic acid composition comprising formic acid from ethane via ethane oxidation.
  • the method for producing acetic acid employs ethane (a gas at ambient temperature and pressure) as a very low cost starting material, which is readily available commercially from the purification of natural gas, or as a side product of many oil refining processes, such as steam cracking of higher hydrocarbons.
  • the ethane is extracted from natural gas.
  • the ethane oxidation step can be carried out in either gas or solution phases, and potentially can employ many potential oxidizing agents for oxidizing ethane such as oxygen gas (which can be alternatively termed diatomic oxygen, or 0 2 ), hydrogen peroxide, inorganic peroxides, organic hydroperoxides, or ozone, or mixtures thereof.
  • oxygen gas which can be alternatively termed diatomic oxygen, or 0 2
  • hydrogen peroxide inorganic peroxides
  • organic hydroperoxides organic hydroperoxides
  • ozone or mixtures thereof.
  • the oxidation is carried out in the gas phase using oxygen and/or air as an oxidant for ethane, optionally with the addition of one or more additional diluent/carrier gases (water/steam, nitrogen, C0 2 , methane, and the like).
  • air is a frequent source for the oxygen gas used to oxidize ethane.
  • air is used as an oxidant, and ethane can be present in an amount ranging from 1 % vol to about 30 % vol of ethane, based on the total volume of the crude acetic acid composition, is mixed with air in order to form a feed stream, including exemplary values of 3 % vol, 5 % vol, 7 % vol, 9 % vol, 10 % vol, 12 % vol, 14 % vol, 16 % vol, 18 % vol, 20 % vol, 22 % vol, 24 % vol, 26 % vol, and 28 % vol.
  • the ethane can be present in an amount ranging from 10 % vol to 20 % vol based on the total volume of the crude acetic acid composition.
  • the ethane oxidation step can be carried out by combining ethane with oxygen and/or or air in the gas phase, then contacting the resulting ethane/oxygen gas mixture with a solid, liquid, or gaseous catalyst, in a reactor at atmospheric or higher pressures, and at elevated temperatures.
  • hydrocarbons such as propane, butanes, pentanes, and hexanes are used as a feedstock for oxidation.
  • the ethane oxidation utilizes a catalyst.
  • catalysts can be employed to improve the rates and selectivity of the ethane oxidation for acetic acid production.
  • a variety of known solid phase catalysts for the gas phase oxidation of ethane to mixtures of acetic acid are known and can be used in the processes described herein.
  • EP 02 94 845 (catalysts comprising Mo x V y Z z wherein z can be nothing or Nb, Sb, Ta, W etc.), EP 04 80 594 (metal oxide catalysts comprising tungsten, vanadium, rhenium, and an alkali metal), EP 04 07 091 (metal oxide catalysts comprising molybdenum, vanadium, rhenium, and an alkali metal), EP 05 18 548 (catalysts having the empirical formula VP a M b O x where M is one or more of Co, Cu, Re, Nb, W, and others), EP 06 27 401 (catalysts having the formula V a Ti b O x ), and WO 99/13980 (metal oxide catalysts having the formula Mo a V b Nb c X d wherein X is selected from P, B, Hf, Te, and As) describe such catalysts for ethane oxidation, and appropriate combinations
  • the catalyst comprises a mixed Mo-V-Nb oxide, and can optionally comprise other metallic components.
  • the reaction product stream from the ethane oxidation can exit the reactor as a vapor stream (the reactor product stream), and can further comprise a mixture of un- reacted ethane and/or oxygen, ethylene (ethene), acetic acid, water vapor, and nitrogen and/or any optional carrier/diluent gases, along with smaller amounts of gases of organic byproducts such as formic acid, ethanal (acetaldehyde), carbon monoxide, and C0 2 , and possibly other heavier organic byproduct compounds in even smaller amounts.
  • This reactor product stream from the ethane oxidation, in the form of a mixed vapor, is not necessarily the crude acetic acid composition described in both steps of the method, which is a liquid steam. Accordingly, in various aspects of the invention, the ethane oxidation step producing the reactor product stream is further processed to an at least partially separate crude acetic acid to produce the liquid crude acetic acid
  • composition which is subjected to purification by crystallization as described.
  • the boiling point of acetic acid is 118-119 °C
  • the boiling point of formic acid is 100.8 °C
  • the boiling point of water is 100 °C
  • the other major components of the reactor product stream ethane, ethylene, oxygen, nitrogen, CO, C0 2 , etc.
  • the reactor product stream vapors from ethane oxidation can be subjected to a cooling/condensation step, to at least partially condense acetic acid, water, and formic acid from the reactor product stream, so as to at least partially and/or substantially separate them from the gases the reactor product stream, such as ethane, oxygen, ethylene, carbon monoxide, carbon dioxide, or nitrogen, or other optional carrier/diluent gases.
  • a cooling/condensation step to at least partially condense acetic acid, water, and formic acid from the reactor product stream, so as to at least partially and/or substantially separate them from the gases the reactor product stream, such as ethane, oxygen, ethylene, carbon monoxide, carbon dioxide, or nitrogen, or other optional carrier/diluent gases.
  • This cooling/condensation step can be carried out at a pressure below the pressure in the oxidation reactor, but at or above atmospheric pressure, and at a temperature slightly below the boiling point of acetic acid at the pressure employed in the cooling/condensation step.
  • a cooling/condensation step can be carried out at atmospheric pressure or slightly above at a temperature between about 118-105 °C, in order to at least somewhat selectively condense acetic acid from the reactor product stream vapors, to produce a liquid crude acetic acid composition that can be further purified as described herein.
  • Such a liquid crude acetic acid composition can comprise a major portion of acetic acid.
  • the crude acetic acid composition comprises water.
  • the crude acetic acid composition further comprises
  • the crude acetic acid composition does not comprise butane, butene, propane, or propylene.
  • the crude acetic acid composition does not comprise ethane, ethylene, butane, propane, propylene, or butene.
  • the butane can be any isomer of butane including n-butane or iso-butane.
  • the butene can be isomer of butene including 1-butene, Z-2-butene, E-2-butene, or iso-butene.
  • Additional optional process steps and/or methods can also be employed to further pre-purify the crude acetic acid composition before it is crystallized.
  • the crude acetic acid composition can optionally be further separated from formic acid, acetaldehyde, and water by a preliminary distillation (in either trayed or packed distillation columns) to produce a crude acetic acid composition comprising only small amounts of water or formic acid, then this pre-purified crude acetic acid composition can be subjected to crystallization.
  • the methods described herein further comprise the step of dehydrating the crude acetic acid composition, often by distillation, though other methods can be used.
  • the purification to remove formic acid and/or water does not comprise a distillation step.
  • the method further comprises one or more steps of dehydrating the crude acetic acid composition to produce a glacial acetic acid.
  • the method further comprises the step of dehydrating the crude acetic acid composition to produce a glacial acetic acid.
  • the method further comprises the step of dehydrating the crude acetic acid composition before the
  • the purity of the crude acetic acid composition produced in the ethane oxidation can vary considerably, though acetic acid can be the major component of the crude acetic acid compositions.
  • the acetic acid component is at least about 50 wt , or at least about 60 wt , or at least about 70 wt , or at least about 80 wt , or at least about 90 wt , or at least about 95 wt , or at least about 98 wt , or at least about 99 wt of the crude acetic acid composition by weight.
  • the formic acid is present in the purified acetic acid composition in an amount less than about 0.2 % by weight, based on the total weight of the purified acetic acid composition.
  • the formic acid is present in the purified acetic acid composition in an amount ranging from 0.001 % by weight to 0.2 % by weight based on the total weight of the purified acetic acid composition, including exemplary values of 0.003 % by weight, 0.005 % by weight, 0.007 % by weight, 0.01 % by weight, 0.03 % by weight, 0.05 % by weight, 0.07 % by weight, 0.09 % by weight, 0.1 % by weight, 0.13 % by weight, 0.15 % by weight, 0.17 % by weight, and 0.19 % by weight.
  • the amount can be in a range derived from any two values.
  • the formic acid can be present in the purified acetic acid composition in an amount ranging from 0.003 % by weight to 0.19 % by weight based on the total weight of the purified acetic acid composition. In some aspects, the formic acid is present in the purified acetic acid composition in an amount less than 0.1 % by weight based on the total weight of the purified acetic acid composition. In another aspect, the formic acid is present in the purified acetic acid composition in an amount less than 0.05 % by weight based on the total weight of the purified acetic acid composition.
  • the formic acid is present in the purified acetic acid composition in an amount less than 0.03 % by weight based on the total weight of the purified acetic acid composition. In an even further aspect, the formic acid is present in the purified acetic acid composition in an amount less than 0.01 % by weight based on the total weight of the purified acetic acid composition.
  • Crystallization also termed fractional crystallization, is a technique well known in the art of purifying organic compounds, both on lab and industrial scales.
  • fractional crystallization describing techniques for various methods of crystallization are available from Sulzer Chemtech of Winterthur Switzerland, a major supplier of industrial crystallization equipment, and are incorporated herein by reference for their description of the major technical factors, techniques, and equipment relevant to purifying organic materials by crystallization.
  • Crystallization of organic chemicals from solvents in general is well known, but not especially useful for purifying acetic acid, whose pure solid crystals melts to the pure liquid not far below room temperature, at the temperature of 16 to 17 °C, and because crystallizing acetic acid from a solution would require very low temperatures.
  • Melt crystallization a technique of fractionally crystallizing organic materials by cooling a relatively pure liquid "melt" of the impure organic material, to form crystals of the material that are purer than the beginning "melt" is suitable for purifying acetic acid herein.
  • fractional/melt crystallization can be suitable for purifying the crude acetic acid compositions produced by the methods described herein. All such forms of fractional crystallization comprise a step of substantially separating at least a portion of crystals comprising acetic acid from the surrounding liquid to form the purified acetic acid composition.
  • Static fractional crystallization involves cooling a static liquid melt of acetic acid, by cooling the walls of the vessel, causing crystals to grow on the walls of the vessel, then draining the remaining liquid to separate the remaining melt from the solid crystals, optionally followed by "sweating" the crystals (as further described below).
  • a phase diagram for such static fractional crystallization separations of water and acetic acid are shown in Figure 1. In some aspects of the methods described herein, the
  • crystallization comprises a step of static fractional crystallization.
  • Falling film crystallization involves distributing a liquid melt of the crude acetic acid composition over a cooled surface, such as the surfaces of a tube, so that crystal formation occurs on the wall of the tube, optionally followed by "sweating" the crystals, then fully melting the crystals on the cooled surface walls to collect the purified acetic acid composition.
  • a cooled surface such as the surfaces of a tube
  • crystallization comprises a step of falling film fractional crystallization.
  • the purity of the purified acetic acid composition produced by any of these fractional crystallization processes can typically be improved by "sweating" the solid acetic acid crystals initially formed and separated from their mother liquors. "Sweating” typically involves an additional step in the fractional crystallization process wherein the separated crystals comprising acetic acid are partially melted and substantially separated from the resulting melted liquid, then the remaining crystals are melted to form the purified acetic acid composition.
  • the crystallization can be performed cooling liquids and forming suspensions of crystals within the liquids.
  • Various methods for collecting such suspended crystals can be used, and can be conducted by various batch wise procedures, such as filtration, or by various continuous processes, such as for example those described by Gerard J. Arkenbout in CHEMTECH, vol.
  • the crude acetic acid composition is subjected to one or more sequences of continuous fractional crystallization to remove water and/or formic acid, by the technique which cools the fraction to freeze out an acetic acid- water eutectic crystalline magma having an acetic acid content higher than the acetic acid content of said fraction, and leaves an acetic acid mother liquor having a water and/or formic acid content higher than the water and/or formic acid content of said fraction, and moves said crystalline magma countercurrent to the flow of the mother liquor, and melts at least a portion of the crystalline magma before its final composition is removed from the fractional crystallization system as product, and moves the melt liquor also countercurrent to the movement of the crystalline magma so that said flowing melt liquor and mother liquor wash the oppositely moving crystalline magma and mix to form a single waste
  • One system can affect such cooling and countercurrent washing by chilling the liquid feed in a long horizontal crystallizer whose inner surfaces, cooled by indirect heat exchange, and are scraped by a helical screw end which advances the crystals as they begin to form near the feed end through to the discharge end.
  • the resulting suspension of crystals in mother liquor discharges into the upper portion of a vertical column having a reciprocating piston periodically pushing down from the top of the column past the entry of the slurry into the column and forcing the slurry downward and then withdrawing toward the top of the column.
  • the column also has, at the upper portion thereof a wall filter which extends from just below entry of the suspension down to slightly below the furthest downward thrust of the piston.
  • the compression of the entering suspension by the piston forces mother liquor through the wall can filter and compact the crystals against the downwardly moving bed of previously compressed crystals.
  • a heating zone can be provided to melt the compacted crystals reaching said heating zone.
  • a valved liquid product exit can be provided in the bottom of the column. The flow of liquid through the valve can be adjusted so that the downwardly moving bed of compacted crystals forces only a part of the melt of the crystals out of the bottom of the column which forces upwardly the remaining portion of the melt of the crystals.
  • the upwardly forced portion of the melt of crystals can flow past the next upward adjacent portion of crystals before they move into the melting zone and can displace mother liquor from and/or melts the outer surfaces of the next upward adjacent portion of crystals, thus forming a new liquid in contact with them of lower impurity content which continues upward displacement of mother liquor from and/or melting outer layers of crystals contacted.
  • new crystals form or crystals grow which can have a lower impurity content.
  • the crude acetic acid composition can be processed to an anhydrous product comprising only extremely low levels of formic acid, as well as only extremely low levels of any heavy end impurities.
  • the temperature required to crystallize acetic acid in such fractional crystallization processes depends on the purity of the crude acetic acid composition and/or its subsequently purified fractions. If the crude acetic acid
  • the acetic acid can be crystallized at a temperature that ranges from about -35°C to about -15°C . If the crude acetic acid composition is moderately impure, the acetic acid can be crystallized at a temperature that ranges from about -15°C to about 17 °C. If the crude acetic acid composition is relatively pure, i.e. above about 95% by weight, the acetic acid is crystallized at a temperature that ranges from about 10 °C to about 17 °C.
  • the purified acetic acid composition comprises total impurities of an amount less than 2 wt %, based on the total weight of the purified acetic acid composition. In some aspects, the purified acetic acid composition comprises total impurities of an amount less than 1 wt %, based on the total weight of the purified acetic acid composition.
  • the purified acetic acid composition comprises total impurities of an amount ranging from 0.001 wt % to 2 wt %, based on the total weight of the purified acetic acid composition, including exemplary values of 0.01 wt %, 0.015 wt %, 0.1 wt %, 0.15 wt %, 0.2 wt %, 0.3 wt %, 0.4 wt %, 0.5 wt %, 0.6 wt %, 0.7 wt %, 0.8 wt %, 0.9 wt %, 1 wt %, 1.2 wt %, 1.4 wt %, 1.6 wt , and 1.8 wt %.
  • the weight percentage can be in a range derived from any two exemplary values.
  • the purified acetic acid composition comprises total impurities of an amount ranging from 0.015 wt % to 1.8 wt % based on the total weight of the purified acetic acid composition.
  • the impurities comprise water, ethane, ethene, ethanal, or formic acid, or combinations thereof.
  • compositions and methods include at least the following aspects.
  • a method for producing acetic acid comprising: producing a crude acetic acid composition comprising formic acid from ethane via ethane oxidation; and then purifying the crude acetic acid composition by crystallization to remove the formic acid to achieve a purified acetic acid composition; wherein the formic acid is present in the purified acetic acid composition in an amount less than 0.2 % by weight, based on the total weight of the purified acetic acid composition.
  • Aspect 2 The method according to aspect 1, wherein the formic acid is present in the purified acetic acid composition in an amount less than 0.1 % by weight, based on the total weight of the purified acetic acid composition.
  • Aspect 3 The method according to aspect 1, wherein the formic acid is present in the purified acetic acid composition in an amount less than 0.05 % by weight, based on the total weight of the purified acetic acid composition.
  • Aspect 4 The method according to aspect 1, wherein the formic acid is present in the purified acetic acid composition in an amount less than 0.03 % by weight, based on the total weight of the purified acetic acid composition.
  • Aspect 5 The method according to aspect 1, wherein the formic acid is present in the purified acetic acid composition in an amount less than 0.01 % by weight, based on the total weight of the purified acetic acid composition.
  • Aspect 6 The method according to any of aspects 1-5, wherein the ethane is extracted from natural gas.
  • Aspect 7 The method according to any of aspects 1-6, wherein the ethane oxidation utilizes 0 2 and/or air as an oxidant.
  • Aspect 8 The method according to any of aspects 1-7, wherein the ethane oxidation utilizes a catalyst.
  • Aspect 9 The method according to aspect 8, wherein the catalyst comprises a mixed Mo-V-Nb oxide.
  • Aspect 10 The method according to any of aspects 1-9, wherein the crude acetic acid composition does not comprise butane, butene, propane, or propylene.
  • Aspect 11 The method according to any of aspects 1-10, wherein the crude acetic acid composition further comprises acetaldehyde.
  • Aspect 12 The method according to any of aspects 1-11, wherein the crude acetic acid composition comprises water.
  • Aspect 13 The method according to any of aspects 1-12, wherein the crude acetic acid composition does not comprise ethane, ethylene, butane, propane, propylene, or butene.
  • Aspect 14 The method according to any of aspects 1-13, wherein the crystallization comprises static fractional crystallization.
  • Aspect 15 The method according to any of aspects 1-13, wherein the crystallization comprises falling film fractional crystallization.
  • Aspect 16 The method according to any of aspects 1-13, wherein the crystallization comprises continuous fractional crystallization.
  • Aspect 17 The method according to any of aspects 1-16, wherein the acetic acid is crystallized at a temperature that ranges from about -35°C to about -15°C.
  • Aspect 18 The method according to any of aspects 1-16, wherein the acetic acid is crystallized at a temperature that ranges from about -15°C to about 17 °C.
  • Aspect 19 The method according to any of aspects 1-16, wherein the acetic acid is crystallized at a temperature that ranges from about 10 °C to about 17 °C.
  • Aspect 20 The method according to any of aspects 1-19, wherein the crystallization comprises a step of substantially separating at least a portion of crystals comprising acetic acid from the surrounding liquid, to form the purified acetic acid composition.
  • Aspect 21 The method according to aspect 20, wherein the separated crystals comprising acetic acid are partially melted and substantially separated from the resulting melted liquid, and then the remaining crystals are melted to form the purified acetic acid composition.
  • Aspect 22 The method according to any of aspects 1-21, wherein the purification to remove formic acid does not comprise a distillation step.
  • Aspect 23 The method according to any of aspects 1-22, wherein the purified acetic acid composition comprises total impurities of an amount less than 2 % by weight, based on the total weight of the purified acetic acid composition.
  • Aspect 24 The method according to any of aspects 1-22, wherein the purified acetic acid composition comprises total impurities of an amount less than 1 % by weight, based on the total weight of the purified acetic acid composition.
  • Aspect 25 The method according to any of aspects 23-24, wherein the impurity comprises water, ethane, ethene, ethanal, or formic acid, or a combination thereof.
  • Aspect 26 The method according to any one of aspects 1-25, wherein the method further comprises the step of dehydrating the crude acetic acid composition.
  • Aspect 27 The method according to any one of aspects 1-26, wherein the method further comprises the step of dehydrating the crude acetic acid composition before the crystallization to remove formic acid.
  • Aspect 28 The method according to any one of aspects 1-27, wherein the method further comprises the step of dehydrating the crude acetic acid composition to produce a glacial acetic acid.
  • Aspect 29 The method according to any one of aspects 1-28, wherein the method further comprises an intermediate step of separating acetic acid from a reactor product stream produced by an ethane oxidation.

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Abstract

Les présentes inventions concernent des procédés de synthèse de l'acide acétique par oxydation de l'éthane, y compris la synthèse de l'acide acétique de pureté élevée comprenant des concentrations très faibles en impureté acide formique. Plus spécifiquement, les présente inventions décrivent des procédés de production d'acide acétique comprenant : a. la production d'une composition d'acide acétique brut comprenant de l'acide formique à partir d'éthane par oxydation de l'éthane ; puis b. la purification de la composition d'acide acétique brut par cristallisation pour éliminer l'acide formique et obtenir une composition d'acide acétique purifié ; l'acide formique étant présent dans la composition d'acide acétique purifié à une teneur inférieure à 0,2 % en masse, par rapport à la masse totale de la composition d'acide acétique purifié.
PCT/US2014/037886 2013-05-13 2014-05-13 Procédés de synthèse de l'acide acétique par oxydation de l'éthane WO2014186386A1 (fr)

Priority Applications (7)

Application Number Priority Date Filing Date Title
AU2014265570A AU2014265570B2 (en) 2013-05-13 2014-05-13 Methods for preparing acetic acid via ethane oxidation
CN201480026054.3A CN105209418B (zh) 2013-05-13 2014-05-13 通过乙烷氧化制备乙酸的方法
US14/787,661 US9738585B2 (en) 2013-05-13 2014-05-13 Methods for preparing acetic acid via ethane oxidation
CA2907955A CA2907955A1 (fr) 2013-05-13 2014-05-13 Procedes de synthese de l'acide acetique par oxydation de l'ethane
EP14730034.7A EP2997003A1 (fr) 2013-05-13 2014-05-13 Procédés de synthèse de l'acide acétique par oxydation de l'éthane
JP2016514040A JP2016523834A (ja) 2013-05-13 2014-05-13 エタン酸化を経て酢酸を調製するための方法
KR1020157031220A KR20160005696A (ko) 2013-05-13 2014-05-13 에탄 산화를 통한 아세트산의 제조 방법

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WO2018209842A1 (fr) * 2017-05-13 2018-11-22 南通宝凯化工有限公司 Procédé de préparation d'acide trifluoroacétique

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CN116574584A (zh) * 2018-01-29 2023-08-11 江苏宇通干燥工程有限公司 高效节能的醋酸连续回收系统
EP3863998A1 (fr) 2018-10-11 2021-08-18 Nova Chemicals (International) S.A. Séparation de composés oxygénés à l'aide d'un sel métallique
US11319265B2 (en) 2018-11-02 2022-05-03 Shell Usa, Inc. Separation of ethane oxidative dehydrogenation effluent
US11492310B2 (en) 2018-11-19 2022-11-08 Nova Chemicals (International) S.A. Oxygenate separation following oxidative dehydrogenation of a lower alkane

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KR20160005696A (ko) 2016-01-15
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JP2016523834A (ja) 2016-08-12
CN105209418B (zh) 2017-03-08
US20160075629A1 (en) 2016-03-17
US9738585B2 (en) 2017-08-22
AU2014265570A1 (en) 2015-10-08
AU2014265570B2 (en) 2016-09-08
EP2997003A1 (fr) 2016-03-23

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